Bad taste in mouth : Anyone with PD get... - Cure Parkinson's

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Bad taste in mouth

Tiger101 profile image
7 Replies

Anyone with PD get bad taste in mouth if so what can be done?

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Tiger101 profile image
Tiger101
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7 Replies

Sour Jacks candy

parkie13 profile image
parkie13

Do you have any clue what is causing it? Medication? Is it coming from your mouth or from your stomach? I'm a firm believer in using 3% hydrogen peroxide in a brown bottle that you buy in a grocery store. I have been using it full strength but if it bothers you you can't diluted with water 50/50. It does the wonderful job killing the bacteria in your mouth.

Tiger101 profile image
Tiger101 in reply toparkie13

Not sure. It’s going along with his loss of taste and smell. He is newly diagnosed with PD and has started Rytary.

alexask profile image
alexask in reply toTiger101

Mannitol restores sense of smell in 80% that have tried it (according to Clinicrowd), so may help with this. It also helps with constipation, so if this is also a problem it is worth a try.

Tiger101 profile image
Tiger101 in reply toalexask

Awesome thanks! My husband has terrible constipation. Maybe goes once a week. He is newly diagnosed so they don't want to introduce anything until he gets used to the Rytary. This is definitely on my list!

alexask profile image
alexask in reply toTiger101

Cool. You can look at my profile for my full regime, but in a nutshell I would recommend - a level tablespoon of Mannitol each morning - ideally in Coffee together with Coconut oil and a low carb breakfast - e.g Bacon and eggs - maybe with one slice of toast. Or a cheese omelette. Take some curcumin with pepper at the same time.

To try and get him moving - apples - eat the core too and crunch the pips as there is some good stuff in there too. Obviously prunes would work too.

I had terrible constipation (from someone who was previously very regular), but this really sorted it.

And exercise as much and varied as possible.

alexask profile image
alexask in reply toalexask

I am 70 kg. With Mannitol you basically need to balance the amount so you become more regular without spending your entire time on the toilet. And not so much in the evening - I got reflux, which may or may not be related. So I don't really have any after about 3pm.

Lot's of people regain their sense of smell with Mannitol, but not much else - but for the early stages I think it can make a major difference in reversing some even many of the symptoms.

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